John D. Overton

Active 2008–2025

96
Papers
20,256
Citations
56
h-index
94
i10-index

Citations

Citations per year for John D. Overton1955: 1 citations1987: 1 citations1991: 1 citations1994: 2 citations2000: 1 citations2004: 2 citations2005: 1 citations2007: 2 citations2009: 7 citations2010: 3 citations2011: 9 citations2012: 52 citations2013: 140 citations2014: 209 citations2015: 176 citations2016: 207 citations2017: 224 citations2018: 256 citations2019: 726 citations2020: 888 citations2021: 1,062 citations2022: 1,111 citations2023: 862 citations2024: 1,257 citations2025: 594 citations2026: 32 citations1956–1986: no citations, so these years are not shown1988–1990: no citations, so these years are not shown1992–1993: no citations, so these years are not shown1995–1999: no citations, so these years are not shown2001–2003: no citations, so these years are not shown2006: no citations, so this year is not shown2008: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,871 citing papers, 26.2% of this breakdownUnited Kingdom: 1,304 citing papers, 8.8% of this breakdownChina: 869 citing papers, 5.9% of this breakdownGermany: 829 citing papers, 5.6% of this breakdownCanada: 630 citing papers, 4.3% of this breakdownItaly: 574 citing papers, 3.9% of this breakdownFrance: 523 citing papers, 3.5% of this breakdownNetherlands: 507 citing papers, 3.4% of this breakdownAustralia: 472 citing papers, 3.2% of this breakdownSweden: 403 citing papers, 2.7% of this breakdownDenmark: 339 citing papers, 2.3% of this breakdownSpain: 336 citing papers, 2.3% of this breakdown
0%26.2%Other 27.9%

Fields

  • Medicine45.5%
  • Biochemistry, Genetics and Molecular Biology41.4%
  • Neuroscience6.3%
  • Immunology and Microbiology3.6%
  • Psychology0.8%
  • Computer Science0.5%
  • Other1.9%

Topics

  • Genetic Associations and Epidemiology6.1%
  • Genomics and Rare Diseases4%
  • Genetics and Neurodevelopmental Disorders2.9%
  • Liver Disease Diagnosis and Treatment2.7%
  • Autism Spectrum Disorder Research2.2%
  • Diabetes, Cardiovascular Risks, and Lipoproteins2%
  • Other80.1%

Coauthors

All papers

Open in search
  1. Exome sequencing and analysis of 454,787 UK Biobank participants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William Salerno, Alan R. Shuldiner, Luca A. Lotta, John D. Overton, Michael Cantor, Jeffrey G. Reid, George D. Yancopoulos, Hyun Min Kang, Jonathan Marchini, Aris Baras, Gonçalo R. Abecasis, Manuel A. R. Ferreira - Nature 2021 cited by 1,077

  2. Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yan V. Sun, Scott L. DuVall, Kelly Cho, Jennifer S. Lee, J. Michael Gaziano, Lawrence S. Phillips, James B. Meigs, Peter D. Reaven, Peter W.F. Wilson, Todd L. Edwards, Daniel J. Rader, Scott M. Damrauer, Christopher J. O’Donnell, Philip S. Tsao, Mark A. Atkinson, Al C. Powers, Ali Naji, Klaus H. Kaestner, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Karina Toledo, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Xiaodong Bai, Suganthi Balasubramanian, Leland Barnard, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Ashish Yadav, Marcus B. Jones, Lyndon J. Mitnaul, VA Million Veteran Program, Samuel M. Aguayo, Sunil K. Ahuja, Zuhair K. Ballas, Sujata Bhushan, Edward J. Boyko, David Cohen, John Concato, Joseph I. Constans, Louis J. Dell’Italia, Joseph Fayad, Ronald Fernando, Hermes Flórez, Melinda A. Gaddy, Saib Gappy and 82 more - Nature Genetics 2020 cited by 801

  3. A Protein-Truncating HSD17B13 Variant and Protection from Chronic Liver Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott M. Damrauer, Daniel J. Rader, Brian Zambrowicz, William C. Olson, Andrew Murphy, Ingrid B. Borecki, Alan R. Shuldiner, Jeffrey G. Reid, John D. Overton, George D. Yancopoulos, Helen H. Hobbs, Jonathan C. Cohen, Omri Gottesman, Tanya M. Teslovich, Aris Baras, Tooraj Mirshahi, Jesper Gromada, Frederick E. Dewey - New England Journal of Medicine 2018 cited by 805

  4. Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laurent F. Thomas, Margo Tuerlings, John Loughlin, Nigel Arden, Fraser Birrell, Andrew Carr, Panos Deloukas, Michael Doherty, Andrew W. McCaskie, William Ollier, Ashok Rai, Stuart H. Ralston, Tim D. Spector, Gillian A. Wallis, Amy E. Martinsen, Cristen J. Willer, Egil A. Fors, Ingunn Mundal, Knut Hagen, Kristian Bernhard Nilsen, Marie Udnesseter Lie, Sigrid Børte, Ben Brumpton, Jonas B. Nielsen, Lars G. Fritsche, Wei Zhou, Ingrid Heuch, Kjersti Storheim, Evangelos Tyrpenou, A. Koukakis, Dimitrios Chytas, Dimitrios Stergios Evangelopoulos, Chronopoulos Efstathios, Spiros G. Pneumaticos, Vasileios S. Nikolaou, Κonstantinos Ν. Malizos, Lydia Anastasopoulou, Gonçalo R. Abecasis, Aris Baras, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Luca A. Lotta, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katia Karalis, Katherine Siminovitch, Christina Beechert, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Michael Lattari, Alexander Lopez, Thomas D. Schleicher, Maria Sotiropoulos Padilla, Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Xiaodong Bai, Suganthi Balasubramanian, Boris Boutkov, Gisu Eom, Lukas Habegger, Alicia Hawes, Olga Krasheninina, Rouel Lanche, Adam J. Mansfield and 55 more - Cell 2021 cited by 467

  5. Common and rare variant associations with clonal haematopoiesis phenotypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Raquel P. Deering, Charles Paulding, Alan R. Shuldiner, Gavin Thurston, Adolfo A. Ferrando, Will Salerno, Jeffrey G. Reid, John D. Overton, Jonathan Marchini, Hyun Min Kang, Aris Baras, Gonçalo R. Abecasis, Eric Jorgenson - Nature 2022 cited by 304

  6. Genetic and Pharmacologic Inactivation of ANGPTL3 and Cardiovascular Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kae‐Woei Liang, Xiuqing Guo, Jerome I. Rotter, Yii‐Der I. Chen, William E. Kraus, Svati H. Shah, Scott M. Damrauer, Aeron Small, Daniel J. Rader, Anders Berg Wulff, Børge G. Nordestgaard, Anne Tybjærg‐Hansen, Anita M. van den Hoek, Hans M.G. Princen, David H. Ledbetter, David J. Carey, John D. Overton, Jeffrey G. Reid, William J. Sasiela, Poulabi Banerjee, Alan R. Shuldiner, Ingrid B. Borecki, Tanya M. Teslovich, George D. Yancopoulos, Scott Mellis, Jesper Gromada, Aris Baras - New England Journal of Medicine 2017 cited by 875

  7. Exome sequencing and characterization of 49,960 individuals in the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Cristen J. Willer, Kristian Hveem, Joseph B. Leader, David J. Carey, David H. Ledbetter, Lon R. Cardon, George D. Yancopoulos, Aris N. Economides, Giovanni Coppola, Alan R. Shuldiner, Suganthi Balasubramanian, Michael Cantor, Matthew R. Nelson, John C. Whittaker, Jeffrey G. Reid, Jonathan Marchini, John D. Overton, Robert A. Scott, Gonçalo R. Abecasis, Laura M. Yerges-Armstrong, Aris Baras - Nature 2020 cited by 636

  8. Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm, Deepika Dokuru, Luke M. Evans, Eco J. C. de Geus, Sudheer Giddaluru, Scott D. Gordon, K. Paige Harden, W. David Hill, Amanda Hughes, Shona M. Kerr, Yongkang Kim, Hyeokmoon Kweon, Antti Latvala, Debbie A. Lawlor, Liming Li, Kuang Lin, Per Magnus, Patrik K. E. Magnusson, Travis T. Mallard, Pekka Martikainen, Melinda C. Mills, Pål R. Njølstad, John D. Overton, Nancy L. Pedersen, David J. Porteous, Jeffrey G. Reid, Karri Silventoinen, Melissa C. Southey, Camilla Stoltenberg, Elliot M. Tucker–Drob, Margaret J. Wright, Hyeokmoon Kweon, Philipp Koellinger, Daniel J. Benjamin, Patrick Turley, Laurence J. Howe, Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho, Geetha Chittoor, Rafael Ahlskog, Penelope A. Lind, Teemu Palviainen, Matthijs D. van der Zee, Rosa Cheesman, Massimo Mangino, Yunzhang Wang, Shuai Li, Lucija Klaric, Scott M. Ratliff, Lawrence F. Bielak, Marianne Nygaard, Alexandros Giannelis, Emily A. Willoughby, Chandra A. Reynolds, Jared V. Balbona, Ole A. Andreassen, Helga Ask, Dorret I. Boomsma, Archie Campbell, Harry Campbell, Zhengming Chen, Paraskevi Christofidou, Elizabeth C. Corfield, Christina C. Dahm and 96 more - Nature Genetics 2022 cited by 393

  9. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2012 cited by 2,183

  10. Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Pablo Kuri‐Morales, Jesús Alegre-Díaz, Jason Torres, Jonathan Emberson, Rory Collins, Suganthi Balasubramanian, Alicia Hawes, Marcus Herbert Jones, Brian Zambrowicz, Andrew Murphy, Charles Paulding, Giovanni Coppola, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Michael Cantor, Hyun Min Kang, Gonçalo R. Abecasis, Katia Karalis, Aris N. Economides, Jonathan Marchini, George D. Yancopoulos, Mark W. Sleeman, Judith Y. Altarejos, Giusy Della Gatta, Roberto Tapia-Conyer, Michal L. Schwartzman, Aris Baras, Manuel A. R. Ferreira, Luca A. Lotta - Science 2021 cited by 276

  11. Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt and 11 more - Nature Genetics 2021 cited by 427

  12. De novo mutations in histone-modifying genes in congenital heart disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , George A. Porter, Amy E. Roberts, Ravi Sachidanandam, Stephan Sanders, Howard Seiden, Mathew W. State, Sai Lakshmi Subramanian, Irina R. Tikhonova, Wei Wang, Dorothy Warburton, Peter S. White, Ismée A. Williams, Hongyu Zhao, Jonathan G. Seidman, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Christine E. Seidman, Richard P. Lifton - Nature 2013 cited by 968

  13. Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Communications 2019 cited by 535

  14. Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alicia Hawes, Marcus B. Jones, Katia Karalis, Shareef Khalid, Olga Krasheninina, Rouel Lanche, Michael Lattari, Dadong Li, Alexander Lopez, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Lyndon J. Mitnaul, Mona Nafde, Jonas B. Nielsen, Sean O’Keeffe, Max Orelus, John D. Overton, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Jeffrey G. Reid, William Salerno, Thomas D. Schleicher, Alan R. Shuldiner, Katherine Siminovitch, Jeffrey Staples, Ricardo H. Ulloa, Niek Verweij, Louis Widom, Sarah E. Wolf, Krishna G. Aragam, Kathryn L. Lunetta, Christopher M. Haggerty, Steven A. Lubitz, Patrick T. Ellinor - Nature Genetics 2022 cited by 173

  15. Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2016 cited by 510

  16. Germline Mutations in CIDEB and Protection against Liver Disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael Cantor, Brian Zambrowicz, Andrew Murphy, Gonçalo R. Abecasis, Manuel A. R. Ferreira, Ēriks Šmagris, Viktoria Gusarova, Mark W. Sleeman, George D. Yancopoulos, Jonathan Marchini, Hyun Min Kang, Katia Karalis, Alan R. Shuldiner, Giusy Della Gatta, Adam E. Locke, Aris Baras, Luca A. Lotta - New England Journal of Medicine 2022 cited by 121

  17. Genomic Analysis of Non- NF2 Meningiomas Reveals Mutations in TRAF7 , KLF4 , AKT1 , and SMO

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel - Science 2013 cited by 904

  18. Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

    Authors: , , , , , , , , , , , , , , - Nature Genetics 2014 cited by 510

  19. Genetic identification of familial hypercholesterolemia within a single U.S. health care system

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Science 2016 cited by 428

  20. Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial

    Authors: , , , , , , , , , , , , , , , , , , , - Circulation 2019 cited by 246

  21. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anthony Marcketta, Matthew S. Lebo, Christina Austin‐Tse, Heather Mason‐Suares, Shannon Bruse, Scott Mellis, Robert S. Phillips, Neil Stahl, Andrew Murphy, Aris N. Economides, Kimberly A. Skelding, Christopher D. Still, James R. Elmore, Ingrid B. Borecki, George D. Yancopoulos, F. Daniel Davis, W. Andrew Faucett, Omri Gottesman, Marylyn D. Ritchie, Alan R. Shuldiner, Jeffrey G. Reid, David H. Ledbetter, Aris Baras, David J. Carey - Science 2016 cited by 607

  22. Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Louis Widom, Sarah E. Wolf, Manasi Pradhan, Kia Manoochehri, Ricardo H. Ulloa, Genome Informatics, Xiaodong Bai, Suganthi Balasubramanian, Andrew Blumenfeld, Gisu Eom, Lukas Habegger, Alicia Hawes, Shareef Khalid, Evan K. Maxwell, William Salerno, Jeffrey Staples, Marcus B. Jones, Lyndon J. Mitnaul, Julia Brosnan, Olle Melander, Sofia Carlsson, Ola Hansson, Tiinamaija Tuomi, Leif Groop, Emma Ahlqvist - Nature Genetics 2021 cited by 175

  23. Genotyping, sequencing and analysis of 140,000 adults from Mexico City

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sebastian Zöllner, Eric Jorgenson, William Salerno, Slavé Petrovski, John D. Overton, Jeffrey G. Reid, Timothy A. Thornton, Gonçalo R. Abecasis, Jaime Berúmen, Lorena Orozco, Rory Collins, RGC Management and Leadership Team, Gonçalo R. Abecasis, Adolfo A. Ferrando, Michael Cantor, Giovanni Coppola, Andrew Deubler, Aris N. Economides, Katia Karalis, Luca A. Lotta, Lyndon J. Mitnaul, John D. Overton, Jeffrey G. Reid, Alan R. Shuldiner, Katherine Siminovitch, Sequencing and Lab Operations, Christina Beechert, Erin D. Brian, Laura M. Cremona, Hang Du, Caitlin Forsythe, Zhenhua Gu, Kristy Guevara, Michael Lattari, Alexander Lopez, Kia Manoochehri, Manasi Pradhan, Raymond Reynoso, Ricardo Schiavo, Maria Sotiropoulos Padilla, Chenggu Wang, Sarah E. Wolf, Amelia Averitt, Nilanjana Banerjee, Dadong Li, Sameer Malhotra, Justin Mower, Mudasar Sarwar, Deepika Sharma, Jeffrey Staples, Jay Sundaram, Sean Yu, Aaron Zhang, Genome Informatics and Data Engineering, Mona Nafde, George Mitra, Sujit Gokhale, Andrew Bunyea, Janice Clauer, Krishna Pawan Punuru, Sanjay Sreeram, Gisu Eom, Benjamin Sultan, Vrushali Mahajan, Eliot Austin, Koteswararao Makkena, Sean O’Keeffe, Tommy Polanco, Ayesha Rasool, William Salerno and 483 more - Nature 2023 cited by 96

  24. Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - JAMA 2019 cited by 158